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    Government

    DC EKG

    Join former White House policy expert Joe Grogan as he cuts through the complexities of healthcare legislation and its real-world implications. Each episode of DC EKG aims to demystify the policies shaping our healthcare system, uncovering how these changes impact patients, providers, and payers across the country.

    Advertise

    Copyright: All Rights Reserved ©2026

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    Latest Episodes:
    "REFILL" | Dr. Brian Miller on FDA Regulatory Reform and the Valley of Death in Medical Innovation (Originally Aired: March 21, 2025) Jul 20, 2026
    Show notes

    In this "Refill" episode, Joe Grogan sits down with Dr. Brian Miller to discuss the "Valley of Death" - the gap between FDA approval and CMS coverage - and how regulatory reform can accelerate medical innovation. Miller explains how FDA product review can be made more efficient through automation and algorithmic analysis of routine tasks, allowing highly trained reviewers to focus on clinical interpretation rather than data processing. The conversation covers clinical trial reform, device review modernization, third-party review programs, and CMS coverage decision processes. Miller argues that these are operational challenges that can be fixed with executive leadership, and that transforming FDA and CMS procedures is critical to bringing new medicines and devices to patients faster.


    Key Timestamps


    1:23 Brian Miller background and AEI role

    2:47 The Valley of Death - gap between FDA approval and CMS coverage

    5:06 Making FDA and CMS review processes more synergistic

    7:43 Example of hypertension drug review and routine tasks

    8:26 Data overload in FDA review process

    10:40 Supplemental applications and unnecessary information

    12:01 FDA reviewer burnout and middle management proliferation

    15:30 Automating routine tasks at FDA

    17:33 Clinical trial reform discussion and regulatory risk

    20:03 Practical approach for new FDA commissioner and DOGE

    21:22 Operational changes needed at FDA

    22:48 Tobacco regulation at FDA and resource allocation

    25:10 Device world getting short shrift in FDA priorities

    27:33 Third-party 510k review program and third-party organizations

    29:09 COVID diagnostic tests and pandemic review process

    30:51 Reforming CDRH through third-party reviews

    31:36 70-year comparison of heart attack treatment advances

    32:46 CMS coverage decisions and Coverage with Evidence Development

    36:02 Medicare Administrative Contractors (MACs) and local coverage decisions

    38:12 Practical market-based approach to MAC appeals

    39:54 National vs local coverage decisions and reasonable and necessary standard

    42:28 Defining reasonable and necessary through algorithms and guidance


    Key Topics

    FDA regulatory reform, Valley of Death, clinical trial reform, FDA product review automation, CMS coverage decisions, Medicare Administrative Contractors, third-party device review, drug development costs, medical innovation, device regulation, regulatory science, operational efficiency


    About the Guest (at time of recording, March 2025)

    Dr. Brian Miller is a physician and non-resident fellow at the American Enterprise Institute (AEI) focusing on FDA regulatory policy and Medicare payment policy. He practices medicine at Johns Hopkins Hospital and serves as an associate professor of medicine and business at Johns Hopkins University. His research and policy work emphasize making regulatory systems more efficient to accelerate the development and approval of innovative medicines and medical devices.


    Podcast: DC EKG with Joe Grogan

    Host: Joe Grogan

    Guest: Dr. Brian Miller


    Sponsor: Survivors for Solutions

    Executive Producer: John CZ Czwartacki, DC EKG Podcast


    "REFILL" | Peter Pitt on FDA Advisory Committees, Make America Healthy Again, and Drug Pricing (Originally Aired: May 23, 2025) Jul 13, 2026
    Show notes

    Joe Grogan sits down with Peter Pitt, FDA veteran and expert on healthcare regulation, to discuss FDA advisory committees, the Make America Healthy Again initiative, and critical gaps in pharmaceutical labeling. Pitt addresses why obesity-related drug dosing information is missing from labels, the importance of vaccine safety, food regulation reform, and strategies for lowering drug prices through generic drug reviews and supply chain diversification. He also discusses the need for FDA and CMS to work together and warns against mission creep at CMS.


    Key Timestamps


    0:44 Background: East Coast native, McGill University, from New York City

    1:07 How he got a professorship at University of Paris School of Medicine

    2:35 Mark McClellan connection and FDA career start

    5:19 Conflicts of interest versus interests in FDA advisory committees

    7:07 Why people need to be dismissed from advisory committees

    9:13 Three basic reasons FDA holds advisory committee meetings

    11:08 Why Canada keeps advisory committees secret versus FDA transparency

    14:08 Advisory committees for CYA, new science, and lack of consensus

    19:44 Op-ed on vaccines and nutrition under Make America Healthy Again

    22:44 Cancer drug dosing for obese patients and missing label information

    27:15 Learning about drug dosing outside of clinical trials

    30:42 Food regulation and FDA's second-class treatment of food safety

    32:02 MAHA moment and removing red food dyes from food supply

    34:00 Dietary supplements regulation under DSHEA

    35:21 Nutrition labeling updates and soda bottle serving sizes

    38:21 PDUFA reauthorization and user fees

    40:32 User fees about predictability not speed

    42:54 CMS mission creep and encroaching on FDA authority


    Key Topics

    FDA advisory committees, transparency, vaccine safety, Make America Healthy Again, pharmaceutical labeling, obesity and drug dosing, food regulation, dietary supplements, generic drug review, PDUFA reauthorization, user fees, CMS mission creep, drug pricing


    About the Guest (at time of recording, May 2025)

    Peter Pitt is President and Co-Founder of the Center for Medicine in the Public Interest and a visiting professor at the University of Paris School of Medicine. He is a former associate commissioner at the FDA where he oversaw advisory committees and served as a senior policy and communications advisor. Pitt is a native of New York City, a McGill University graduate, and speaks fluent French.


    Podcast: DC EKG with Joe Grogan

    Host: Joe Grogan

    Guest: Peter Pitt


    Sponsor: Survivors for Solutions

    Executive Producer: John CZ Czwartacki, DC EKG Podcast


    "REFILL" - Ryan Long on the ACA Subsidy Fight, Phantom Enrollees, and Reforming 340B Jul 06, 2026
    Show notes

    Podcast TitleDC EKG with Joe Grogan: A Healthcare Policy Podcast


    This is a REFILL of Episode124 - (Original air date: January 27, 2026)


    Episode Title - Ryan Long on the ACA Subsidy Fight, Phantom Enrollees, and Reforming 340B


    Episode Description - Joe Grogan is joined by Ryan Long of Paragon Health Institute and the University of Southern California to break down two fights shaping health policy right now: a California wealth tax pitch framed as a health care fix, and the battle over extending enhanced Affordable Care Act subsidies.


    They unpack how enhanced subsidies changed who qualifies, why zero-premium plans opened the door to broker-driven enrollment and fraud, and why the medical loss ratio creates perverse incentives that can push premiums higher. They also explain how silver loading and cost-sharing reduction policy distort the exchange market, and what reforms could lower costs without writing a blank check.


    The episode closes with Ryan's latest work on the 340B program, including why drug arbitrage rewards hospitals with a stronger commercial mix and can fuel consolidation, and why direct, targeted assistance could better support hospitals that truly serve low-income and rural patients.


    Chapters and Timestamps

    00:01 Intro

    00:23 Welcome, and what is on the agenda

    01:25 California wealth tax and structural deficits

    11:20 Enhanced ACA subsidies and the shutdown fight

    16:54 Income caps, zero premium plans, and phantom enrollees

    21:50 Fraud, Medicaid exposure, and public trust

    30:39 Medical loss ratio incentives and ACA market fixes

    38:41 340B: how arbitrage works and why it drives consolidation

    44:51 What reform could look like

    47:20 Closing


    SEO Keywords | Affordable Care Act, ACA subsidies, enhanced subsidies, premium tax credits, exchange plans, zero premium plans, phantom enrollees, medical loss ratio, cost sharing reduction, silver loading, Medicaid fraud, Minnesota fraud, California wealth tax, 340B program, drug arbitrage, hospital consolidation, site neutral payments, commercial mix, Medicare Trust Fund


    About Our Guest | Ryan Long is a health policy expert with experience on Capitol Hill, including years in the Speaker's office and on the House Energy and Commerce Committee. He is affiliated with Paragon Health Institute and the University of Southern California.


    CreditsSponsor: Survivors for SolutionsExecutive Producer: John “CZ” Czwartacki, DC EKG PodcastProducer: Julie Riga, Stay on Course Studios, https://www.stayoncourse.studio


    "REFILL" White House Rivalries and CDC Reform with Dr. Tevi Troy Jun 29, 2026
    Show notes

    An episode pulled from the archives, Joe Grogan and Eric Ueland welcome Dr. Tevi Troy, former Deputy Secretary of Health and Human Services, presidential historian, and best selling author of Fight House: Rivalries in the White House from Truman to Trump. First aired in February 2023 at the midpoint of the Biden administration, this conversation diagnoses how White House infighting actually works, why the Biden team leaked so much less than its predecessors, and what discipline does and does not buy a president.

    From there the conversation turns to the machinery of the State of the Union, why the speech always collapses into a laundry list, and how Ronald Reagan invented the pageantry that every president has copied since. Troy then makes the bipartisan case for reforming the Centers for Disease Control, arguing for a congressional charter and a sharper pandemic mission separate from behavioral health. Along the way Joe, Eric, and Tevi cover Lyndon Johnson and Vietnam, Ed Koch and the art of criticizing opponents without alienating voters, the real origin of the Bull Connor line in Biden speeches, and why Troy believes the Republican party has a brighter future after Trump than the Democrats have after Biden.


    TIMESTAMPS

    0:00 Tevi Troy on a brighter Republican future after Trump

    0:47 DC EKG intro

    1:10 Joe and Eric welcome Tevi Troy, refill context from February 2023

    3:00 Why the Biden White House leaks far less than Trump's did

    6:15 Neera Tanden, Afghanistan, and where the grumbling did surface

    9:30 Is the press softer on Democratic administrations

    12:10 Lessons from the hyper disciplined Bush 43 operation

    15:00 Friction as a feature: Johnson, Ford, and creative tension

    18:20 Johnson, Vietnam, and the limits of dominating Congress

    21:00 Biden faces a Republican House and a debt ceiling fight

    24:15 How a State of the Union actually gets built

    27:30 Why every State of the Union becomes a laundry list

    30:45 Reagan, Lenny Skutnik, and the birth of pageantry

    33:50 The case for reforming the CDC with a congressional charter

    36:20 Behavioral health versus the pandemic mission

    39:10 Ed Koch, Carter, and criticizing without alienating voters

    41:40 Where Meacham's Bull Connor line came from

    44:30 Troy's path to DC: AEI, Ben Wattenberg, and the PhD

    47:15 The conservative movement in flux and the future of the parties

    48:33 Wrap up


    ABOUT OUR GUEST

    Dr. Tevi Troy is a presidential historian, best selling author, and former Deputy Secretary of the Department of Health and Human Services. An insider's insider in Washington, he warned of US vulnerability to coronavirus in 2016 and has since written widely on the failures at the CDC. He began his career at the American Enterprise Institute working for Ben Wattenberg, earned a PhD from the University of Texas at Austin, and served in a range of roles in the George W. Bush administration, including at the Domestic Policy Council. He is the author of Fight House: Rivalries in the White House from Truman to Trump, What Jefferson Read, Ike Watched, and Obama Tweeted, and Intellectuals and the American Presidency, along with more than four hundred articles.


    CREDITS

    Podcast: DC EKG with Joe Grogan

    Episode: 137b

    Guest: Dr. Tevi Troy, former Deputy Secretary of Health and Human Services

    Sponsor: Survivors for Solutions, https://survivorsforsolutions.org

    Executive Producer: John “CZ” Czwartacki, DC EKG Podcast

    Producer: Stay on Course Studios, https://www.stayoncourse.studio


    "REFILL" | Dr. Jay Bhattacharya on COVID Infection Rates, Natural Immunity, and the Great Barrington Declaration (Originally Aired: July 20, 2023) Jun 22, 2026
    Show notes

    Dr. Jay Bhattacharya on COVID-19 Seroprevalence, Natural Immunity, and the Great Barrington Declaration (Originally Aired July 20, 2023)


    This episode originally aired on July 20, 2023, the same day Stanford University President Tessier-Levine was forced to resign. Dr. Jay offers detailed commentary on the hostile work environment at Stanford and how government, big tech, and academia conspired to suppress scientific voices.


    Episode Description

    In this wide-ranging conversation, Joe Grogan and Eric Ueland sit down with Dr. Jay Bhattacharya to discuss his groundbreaking work on COVID-19 seroprevalence studies, the suppression of natural immunity data, and the origins of the Great Barrington Declaration.


    Dr. Bhattacharya shares his immigrant family story and early recognition that COVID-19 was far more widespread than official counts indicated. He conducted one of the first seroprevalence studies in April 2020 in Santa Clara and Los Angeles Counties, using antibody test kits provided by Major League Baseball, and found that the disease was 40 to 50 times more common than reported cases.


    The episode covers the intense backlash Dr. Bhattacharya faced for publishing these findings, including death threats, racist attacks, and institutional pressure from Stanford to suppress the research. He discusses how public health authorities suppressed evidence of natural immunity, the unethical decision-making by officials like Tony Fauci and Debbie Birx, and the formation of the Great Barrington Declaration.


    Dr. Bhattacharya details the coordinated campaign against him, censorship on social media, including Twitter blacklisting, federal government threats to ensure censorship, and the terrible price paid that will echo through generations. He reflects on the failures of scientific institutions and the reforms needed to restore public trust in science.


    Key Timestamps


    4:27 Background: born in India, immigrant family, father was a rocket scientist

    14:07 COVID enters consciousness: late December 2019, early January 2020

    16:47 Wall Street Journal op-ed calling for seroprevalence studies

    19:06 Major League Baseball provides 10,000 antibody test kits

    20:30 Study results: 3 percent of Santa Clara had COVID by April 2020

    26:12 Death threats, racist attacks, and pressure from Stanford

    34:51 Evidence of natural immunity being suppressed by Fauci and Birx

    39:52 Genesis of Great Barrington Declaration, October 2020

    50:10 Hostile work environment at Stanford and Tessier-Levine impact

    56:44 FOIA requests revealing government targeting

    1:00:16 Twitter blocklist discovery and Elon Musk's Twitter Files

    1:05:00 Reform is needed in the scientific community to restore public trust


    About the Guest (at time of recording, July 2023)

    Dr. Jayanta Jay Bhattacharya is a Professor of Health Policy at Stanford University's School of Medicine and a Senior Fellow at the Hoover Institution. He holds an MD and a PhD in Economics from Stanford. Born in Kolkata, India, he immigrated to the US at age four. His research focuses on the health and well-being of vulnerable populations. He has published over 160 peer-reviewed articles and is the author of a leading textbook on health economics. Dr. Bhattacharya co-authored the Great Barrington Declaration and is a co-founder of the Academy of Science and Freedom.


    Dr. Jay's Current Role (June 2026)

    Since this episode was recorded in July 2023, Dr. Bhattacharya has assumed significant leadership roles in the federal government. He is the 18th Director of the National Institutes of Health (NIH), confirmed March 25, 2025, and took office April 1, 2025. As of February 18, 2026, he also serves as Acting Director of the Centers for Disease Control and Prevention (CDC), bringing his emphasis on scientific integrity and evidence-based policy to these critical positions.


    Podcast: DC EKG with Joe Grogan

    Guest: Dr. Jay Bhattacharya

    Host: Joe Grogan and Eric Ueland


    Sponsor: Survivors for Solutions

    Executive Producer: John CZ


    Tax Expenditures, 340 B Drug Pricing, and Kidney Donation Reform Jun 15, 2026
    Show notes

    DC EKG with Joe Grogan

    Episode 137: Tax Expenditures, 340 B Drug Pricing, and Kidney Donation Reform

    Air Date: June 15, 2026

    Episode Description

    In this episode, Joe Grogan sits down with Dr. Ike Brannon, President of Capital Policy Analytics and Senior Fellow at the Jack Kemp Foundation, to discuss hidden tax expenditures, the 340 B drug pricing program, and innovative solutions to the kidney shortage crisis.

    Dr. Brannon brings decades of Capitol Hill experience, including roles as chief economist of the House Energy and Commerce Committee and senior advisor to Senator Orrin Hatch. He and co-author Tony LoSasso recently published groundbreaking research in Health Affairs Forefront arguing that the 340 B drug pricing program should be classified as a hidden tax expenditure costing the federal government 15 to 20 billion dollars annually.

    The conversation covers how the 340 B program evolved from providing discounted drugs to uninsured patients into a massive subsidy for nonprofit institutions with little benefit to poor patients. Dr. Brannon explains how the same drug acquired at a 340 B discount often results in full commercial copays for patients.

    Joe and Dr. Brannon explore other problematic tax expenditures including the mortgage interest deduction, employer health insurance exclusion, and credit union tax breaks. The episode pivots to Dr. Branons passionate work on kidney donation reform. Forty-five thousand Americans die annually from end stage renal failure due to kidney shortage, disproportionately affecting African Americans. Dr. Brannon advocates for fully reimbursing kidney donors for all expenses.

    Key Topics

    340 B drug pricing program, tax expenditures, pharmaceutical discounts, nonprofit hospitals, mortgage interest deduction, kidney donation, end stage renal failure, organ shortage, entitlement reform, social security, Medicare, federal deficit, health economics

    Key Timestamps

    0:00 Opening: What should be in a reconciliation bill?

    4:38 The 340 B drug pricing program explained

    13:54 How the 340 B discount does not reach patients

    20:13 Mortgage interest deduction: the most irritating tax break

    31:00 Prospects for reconciliation under Trump administration

    34:57 The kidney donation crisis: 45,000 deaths per year

    39:02 How kidney donation reimbursement would work

    40:00 Would you allow kidney sales? The ethical debate

    45:13 Final thoughts

    About the Guest

    Dr. Ike Brannon is President of Capital Policy Analytics and Senior Fellow at the Jack Kemp Foundation. He holds a PhD in Economics from Indiana University. Dr. Brannon served as chief economist of the House Energy and Commerce Committee, senior advisor to Senator Orrin Hatch on tax and trade policy, and has worked at the Congressional Joint Economic Committee, Treasury Department, and for the McCain presidential campaign. He is founder of the Prosperity Caucus and focuses on growth-oriented economic policy and healthcare innovation.

    Featured Research

    The 340 B Drug Pricing Program is a Hidden Tax Expenditure

    Health Affairs Forefront, April 24, 2026

    Co-authored by Ike Brannon and Tony LoSasso

    https://www.healthaffairs.org/content/forefront/340b-drug-pricing-program-hidden-tax-expenditure

    Podcast: DC EKG with Joe Grogan

    Episode: 137

    Guest: Dr. Ike Brannon

    Sponsor: Survivors for Solutions

    Producer: Stay on Course Studios

    Executive Producer: John CZ Czwartacki, DC EKG Podcast



    "REFILL" - The Economics of Ozempic and Other Weight Loss Drugs (Originally Aired: May 2024) Jun 08, 2026
    Show notes

    DC EKG with Joe Grogan

    The Economics of Ozempic and Other Weight Loss Drugs

    Episode 136.5 (“Prescription Refill” – A replay from the archives)

    Original Air Date: May 2024


    In this episode, Joe Grogan welcomes Ben Ippolito, Senior Fellow in Economic Policy Studies at the American Enterprise Institute, to discuss the rapidly evolving economics of GLP-1 weight loss drugs like Ozempic and Wegovy.


    Ben explains the two main competitors in this market—Novo Nordisk's Ozempic and Wegovy versus Eli Lilly's Mounjaro and Zepbound. Revealing how insurance coverage decisions drive pharmaceutical marketing strategy.


    The conversation reveals a critical irrationality in Medicare policy: the statutory prohibition on covering weight loss drugs despite their profound clinical and quality-of-life benefits. Yet these same drugs are covered for diabetes and cardiovascular risk reduction.


    Ben explores the surprising economics of drug pricing through gross-to-net pricing—the massive gap between list prices and what insurers actually pay through rebates and discounts.


    The episode examines critical implications of the Inflation Reduction Act's price negotiation provisions. Once Medicare negotiates Ozempic's price, that same price applies to all products using the same active ingredient. This creates cascading market effects: competitors must match those prices to remain on formularies, new entrants face lower pricing power even if clinically superior, and pharmaceutical companies may abandon promising programs due to regulatory uncertainty.


    Ben argues Congress doesn't need to act immediately to expand Medicare coverage, but likely will within a few years.


    Joe and Ben discuss unintended consequences of government price regulation, including effects on innovation and drug development pipelines. They explore how price controls announced before elections affect pharmaceutical strategy and development timelines.


    Concluding with Ben's research on Medicare Advantage and why both Democrats and Republicans scrutinize this private alternative to traditional Medicare. With over 50 percent of seniors enrolled in Medicare Advantage plans, bipartisan interest in reform is reshaping healthcare policy conversations on Capitol Hill.


    Key Topics

    GLP-1 drugs, Ozempic, Wegovy, Mounjaro, Zepbound, weight loss medications, obesity treatment, Medicare coverage, drug pricing, Inflation Reduction Act, pharmaceutical competition, rebates, gross-to-net pricing, health economics, cardiovascular benefits, diabetes treatment, Medicare Advantage, healthcare policy, innovation incentives



    Key Timestamps

    00:00 Cold Open: "Turned Up to 11"

    00:24 Welcome to DC EKG

    00:46 Meet Ben Ippolito (AEI)

    03:48 The GLP-1 Landscape: Ozempic, Wegovy, and the Field

    05:04 One Drug, Two Names

    06:45 Medicare's Weight-Loss Coverage Ban

    07:21 Blockbusters and Big Effect Sizes

    09:32 Why Isn't Congress Acting?

    10:17 Why It Costs Less Than You Think

    12:34 The Coverage Irrationality

    14:05 Quality of Life as a Real Benefit

    15:17 Beyond Weight: Cravings and Addiction

    18:21 Devil's Advocate: Why Cover It At All?

    19:48 Gross-to-Net and the Rebate Problem

    22:41 Why Can't You Just Pay Cash?

    25:43 The IRA and the Ozempic Price Cut

    27:32 One Ingredient, One Price

    30:10 Unintended Consequences in Part D

    34:01 New Competitors and Killed Programs

    38:03 What's Next: Medicare Advantage

    42:04 Wrap-Up and Credits


    About the Guest

    (As of May 2024) Ben Ippolito is a Senior Fellow in Economic Policy Studies at the American Enterprise Institute. He holds a PhD and Master's degree in Economics from the University of Wisconsin-Madison and a Bachelor's degree in Mathematics and Economics from Emory University. Ben examines drug pricing policy, Medicare Advantage, and healthcare innovation economics with regular engagement with Congress.


    Podcast: DC EKG with Joe Grogan

    Guest: Ben Ippolito


    Sponsor: Survivors for Solutions

    Producer: Stay on Course Studios

    Executive Producer: John CZ Czwartacki, DC EKG Podcast


    Tom Barker on The Truth About Drug Pricing Policy Jun 01, 2026
    Show notes

    In Episode 136 of DC EKG, Joe Grogan hosts Tom Barker, a top drug-pricing attorney at Foley Hoag and former acting general counsel of Health and Human Services (HHS) under the Bush administration. Tom helped implement Medicare Part D and now advises drugmakers and policymakers on complex pricing issues. The episode traces 20 years of policy: what went right with Part D, what the Inflation Reduction Act (IRA) did, and what effective policy should look like.


    Tom explains that Part D's success rested on three pillars: private plans only, limited government control over benefit design, and a non-interference clause barring the government from intervening in negotiations among plans, pharmacies, and manufacturers. Competition worked and premiums stayed low, until the government asserted more control and weakened those pillars. The IRA, he argues, was a 16-year Democratic effort to repeal non-interference, creating price controls disguised as negotiations.

    The Trump administration has taken a different tack, focusing not on the IRA but on MFN and Globe Guard models pegged to other developed countries. Tom also breaks down the 340B program, now the country's second-largest expenditure program, and the fight between manufacturers and covered entities over contract pharmacies.


    His prescription is simple: let competition work. Speed FDA approval of generics and biosimilars, and trust the marketplace over price controls. He points to hepatitis C, where prices fell sharply once competition entered.


    In This Conversation

    The three pillars that made Part D successful for 20 years

    How non-interference kept government from setting drug prices

    The IRA as a 16-year Democratic push to repeal non-interference

    Why Tom calls the IRA price controls disguised as negotiations

    The Trump administration's focus on MFN and Globe Guard pricing

    340B and the battle between manufacturers and covered entities

    The Chevron repeal's impact on drug pricing law

    HRSA's proposed rebate model and ongoing 340B litigation

    Why effective policy means competition, not controls

    Tom's work helping North Korean defectors and refugees


    Key Timestamps

    1:51 Tom's background at HHS and CMS

    2:30 The three pillars of Part D's success

    5:10 Why Democrats wanted to repeal non-interference

    5:55 Ted Kennedy's compromise and bipartisan votes

    11:38 The IRA as a 16-year repeal attempt

    12:03 What the IRA changed in Part D

    15:02 IRA negotiations vs. real negotiations

    16:25 How the excise tax makes it no real negotiation

    21:32 Trump's focus on MFN and Globe Guard

    25:37 340B's history back to 1991

    28:45 340B as the second-biggest expenditure program

    29:30 Manufacturer vs. covered-entity acrimony

    33:18 The Chevron repeal's impact on pricing

    34:54 HRSA's rebate model, the next step on 340B

    35:40 The lawsuit over "patient" in 340B

    38:18 Tom's advice: let competition work

    39:30 Hepatitis C: competition drives prices down

    40:34 Competition for gene therapies and CRISPR

    41:36 Tom's work for North Korean defectors

    44:49 Sponsoring Free North Korea Radio


    Medicare Part D, drug pricing policy, Inflation Reduction Act, non-interference clause, 340B program, MFN pricing, Globe Guard pricing, pharmacy benefit managers, covered entities, contract pharmacies, biosimilars, generics, federal drug pricing, government price controls, Tom Barker


    About the Guest

    Tom Barker is a partner at Foley Hoag in Washington, DC, and one of the country's top drug pricing attorneys. He served as acting general counsel of HHS and chief legal officer at CMS under the Bush administration, where he helped implement Part D from its inception. He is now a go-to expert on drug pricing, and helps North Korean defectors navigate US immigration law.


    Podcast: DC EKG with Joe Grogan

    Episode: 136 Guest: Tom Barker

    Sponsor: Survivors for Solutions - https://survivorsforsolutions.org

    Executive Producer: John "CZ" Czwartacki,

    DC EKG Podcast Producer: Stay on Course Studios - https://www.stayoncourse.studio


    Dr. Mark McClellan on How FDA and CMS Should Work Together May 25, 2026
    Show notes



    Dr. Redfield's Warning: Hantavirus| Bird Flu| Long COVID and More May 18, 2026
    Show notes

    In Episode 134 of DC EKG, former CDC Director Dr. Robert Redfield joins Joe Grogan to discuss his new book, Redfield's Warning, and break down three major threats to public health: Long COVID, Hantavirus, and bird flu. Dr. Redfield explains the persistent viral reservoirs in long COVID patients, the cognitive dysfunction and autonomic dysfunction that devastate these individuals, and why the federal government must partner with the private sector to develop meaningful treatments. He also walks through the current Hantavirus outbreak on a cruise ship, the human-to-human transmission of the Andes virus strain, and why bird flu is the most likely candidate for the next pandemic. Throughout, Dr. Redfield emphasizes the critical importance of antiviral development and the dangers of gain-of-function research.


    In This Conversation


    The current Hantavirus outbreak on a cruise ship and human-to-human transmission


    The Andes virus strain and why it differs from Sin Nombre and Four Corners Disease


    Two transmission routes: aerosolization and direct contamination


    Asymptomatic transmission and the intrinsic bias in testing


    Why has the US government not developed Hantavirus countermeasures in 70 years


    Bird flu is the most likely candidate for the next pandemic.


    Gain-of-function research and the public disclosure of dangerous genetic data


    Long COVID: viral reservoirs and the need for effective antiviral treatments


    Why antivirals should be the priority over vaccines for emerging viruses


    Operation Warp Speed and the importance of private sector partnerships


    The dismissal of long COVID patients as psychosomatic and the need for validation


    Key Timestamps

    1:49 Details of the Hantavirus outbreak and cruise ship cases

    3:00 Two methods of transmission: aerosolization and direct contamination

    5:24 Asymptomatic transmission and testing bias

    10:35 The Hantavirus family and why the Andes virus goes from human to human

    12:35 How nervous should the public be

    16:43 Shifting to bird flu and Redfield's Warning

    19:00 Bird flu spread in US poultry and mammal populations

    22:00 The four amino acids for bird flu to infect humans

    23:30 The debate with Fauci over gain-of-function research

    27:55 Unregulated gain-of-function research worldwide

    33:35 Why antivirals should be the priority

    37:55 Long COVID viral reservoirs and treatment gaps

    42:37 The economic burden and need for solutions

    43:57 The story of Joy and psychiatric misdiagnosis of long COVID

    48:12 The solvability of long COVID and the importance of investing


    Hantavirus, Hantavirus transmission, Andes virus, Sin Nombre virus, Four Corners Disease, cruise ship outbreak, bird flu, avian influenza, gain of function research, Dr. Robert Redfield, CDC Director, antivirals, vaccines, long COVID, pandemic preparedness, infectious disease, virology, Redfield's Warning


    About the Guest

    Dr. Robert Redfield is the former Director of the Centers for Disease Control and Prevention. A trained virologist with decades of experience in infectious disease, he has been a leading voice on public health policy, pandemic preparedness, and biosecurity. He is the author of Redfield's Warning: What I Learned as CDC Director and What We Must Do to Be Prepared for the Next Pandemic, available on Amazon: https://www.amazon.com/Redfields-Warning-Learned-Couldnt-Might/dp/1510785051


    Podcast: DC EKG with Joe Grogan

    Episode: 134

    Guest: Dr. Robert Redfield, former CDC Director

    Sponsor: Survivors for Solutions –

    https://survivorsforsolutions.org

    Executive Producer: John "CZ" Czwartacki, DC EKG Podcast

    Producer: Stay on Course Studios –

    https://www.stayoncourse.studio



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